US4842834A - Process for reducing the concentration of pollutants in an effluent - Google Patents
Process for reducing the concentration of pollutants in an effluent Download PDFInfo
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- US4842834A US4842834A US07/009,696 US969687A US4842834A US 4842834 A US4842834 A US 4842834A US 969687 A US969687 A US 969687A US 4842834 A US4842834 A US 4842834A
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- effluent
- atomization
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- supply
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- 238000000034 method Methods 0.000 title claims abstract description 27
- 239000003344 environmental pollutant Substances 0.000 title abstract description 9
- 231100000719 pollutant Toxicity 0.000 title abstract description 9
- 238000000889 atomisation Methods 0.000 claims abstract description 77
- 239000012530 fluid Substances 0.000 claims abstract description 60
- 239000000446 fuel Substances 0.000 claims abstract description 14
- 238000002485 combustion reaction Methods 0.000 claims abstract description 12
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 claims description 94
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 21
- 239000004202 carbamide Substances 0.000 claims description 21
- 239000000654 additive Substances 0.000 claims description 11
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- 238000001816 cooling Methods 0.000 claims description 7
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- 230000000694 effects Effects 0.000 claims description 4
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- 239000007924 injection Substances 0.000 abstract description 13
- 238000009826 distribution Methods 0.000 abstract description 3
- 239000000243 solution Substances 0.000 description 22
- 150000001875 compounds Chemical class 0.000 description 14
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- 239000000523 sample Substances 0.000 description 10
- 239000006185 dispersion Substances 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 8
- 229910021529 ammonia Inorganic materials 0.000 description 6
- 239000000463 material Substances 0.000 description 6
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- 239000004312 hexamethylene tetramine Substances 0.000 description 4
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- 229910002091 carbon monoxide Inorganic materials 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
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- 239000004215 Carbon black (E152) Substances 0.000 description 2
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- 239000011149 active material Substances 0.000 description 2
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- 238000004519 manufacturing process Methods 0.000 description 2
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- 229910052815 sulfur oxide Inorganic materials 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- KNIKDPRISVIPBU-UHFFFAOYSA-N 1,2-dichloro-4-[isocyano-(4-methylphenyl)sulfonylmethyl]benzene Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C([N+]#[C-])C1=CC=C(Cl)C(Cl)=C1 KNIKDPRISVIPBU-UHFFFAOYSA-N 0.000 description 1
- MVXMNHYVCLMLDD-UHFFFAOYSA-N 4-methoxynaphthalene-1-carbaldehyde Chemical compound C1=CC=C2C(OC)=CC=C(C=O)C2=C1 MVXMNHYVCLMLDD-UHFFFAOYSA-N 0.000 description 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- XNCOSPRUTUOJCJ-UHFFFAOYSA-N Biguanide Chemical compound NC(N)=NC(N)=N XNCOSPRUTUOJCJ-UHFFFAOYSA-N 0.000 description 1
- 229940123208 Biguanide Drugs 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- MGJKQDOBUOMPEZ-UHFFFAOYSA-N N,N'-dimethylurea Chemical compound CNC(=O)NC MGJKQDOBUOMPEZ-UHFFFAOYSA-N 0.000 description 1
- VGGLHLAESQEWCR-UHFFFAOYSA-N N-(hydroxymethyl)urea Chemical compound NC(=O)NCO VGGLHLAESQEWCR-UHFFFAOYSA-N 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- XGEGHDBEHXKFPX-UHFFFAOYSA-N N-methylthiourea Natural products CNC(N)=O XGEGHDBEHXKFPX-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000003916 acid precipitation Methods 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 235000012501 ammonium carbonate Nutrition 0.000 description 1
- VZTDIZULWFCMLS-UHFFFAOYSA-N ammonium formate Chemical compound [NH4+].[O-]C=O VZTDIZULWFCMLS-UHFFFAOYSA-N 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- VBIXEXWLHSRNKB-UHFFFAOYSA-N ammonium oxalate Chemical compound [NH4+].[NH4+].[O-]C(=O)C([O-])=O VBIXEXWLHSRNKB-UHFFFAOYSA-N 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 1
- 238000009529 body temperature measurement Methods 0.000 description 1
- STIAPHVBRDNOAJ-UHFFFAOYSA-N carbamimidoylazanium;carbonate Chemical compound NC(N)=N.NC(N)=N.OC(O)=O STIAPHVBRDNOAJ-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
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- 230000006835 compression Effects 0.000 description 1
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- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- TXKMVPPZCYKFAC-UHFFFAOYSA-N disulfur monoxide Inorganic materials O=S=S TXKMVPPZCYKFAC-UHFFFAOYSA-N 0.000 description 1
- 239000002803 fossil fuel Substances 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 description 1
- JWZCAURPOJBWGI-UHFFFAOYSA-N hydroxymethylurea;urea Chemical compound NC(N)=O.NC(=O)NCO JWZCAURPOJBWGI-UHFFFAOYSA-N 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000002085 irritant Substances 0.000 description 1
- 231100000021 irritant Toxicity 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- XGEGHDBEHXKFPX-NJFSPNSNSA-N methylurea Chemical compound [14CH3]NC(N)=O XGEGHDBEHXKFPX-NJFSPNSNSA-N 0.000 description 1
- 239000010743 number 2 fuel oil Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- QUBQYFYWUJJAAK-UHFFFAOYSA-N oxymethurea Chemical compound OCNC(=O)NCO QUBQYFYWUJJAAK-UHFFFAOYSA-N 0.000 description 1
- 229950005308 oxymethurea Drugs 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
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- 239000002243 precursor Substances 0.000 description 1
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- 150000003254 radicals Chemical class 0.000 description 1
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- 238000005201 scrubbing Methods 0.000 description 1
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Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/46—Removing components of defined structure
- B01D53/54—Nitrogen compounds
- B01D53/56—Nitrogen oxides
Definitions
- the present invention relates to the reduction of pollutants, such as nitrogen oxides in an effluent, from the combustion of a carbonaceous fuel. More particularly, this invention relates to a process and apparatus therefor.
- Carbonaceous fuels can be made to burn more completely, and with reduced emissions of carbon monoxide and unburned hydrocarbons, when the oxygen concentrations and air/fuel ratios employed are those which permit high flame temperatures.
- high flame temperatures it is meant that, for instance, when fossil fuels are used to fire large utility boilers, temperatures above about 2000° F. and typically about 2200° F. to about 3000° F. are generated.
- thermal NO x the temperatures being so high that free radicals of oxygen and nitrogen are formed and chemically combined as nitrogen oxides (NO x ).
- Nitrogen oxides are troublesome pollutants which are found in the combustion effluent streams of large utility boilers when fired as discussed above, and comprise a major irritant in smog. It is further believed that NO x compounds can undergo a process known as photo-chemical smog formation, through a series of reactions, in the presence of sunlight and hydrocarbons. Moreover, nitrogen oxides comprise a major portion of acid rain.
- Williamson discloses the purification of acid gas-containing streams at low temperatures approaching ambient by contacting the gas stream with an amine vapor in sufficient concentration such that its partial pressure is at least 5% of the total pressure of the gas stream.
- Bowers in copending and commonly assigned U.S. patent application, Ser. No. 784,826, filed Oct. 4, 1985, and copending and commonly assigned U.S. patent application, Ser. No. 811,532, filed Dec. 20, 1985, discloses the use of a urea solution, which preferably also comprises hexamethylenetetramine, to reduce the NO x concentration in the effluent of a carbonaceous fuel.
- a urea solution which preferably also comprises hexamethylenetetramine
- compositions which are effective at reducing the NO x concentrations in an effluent while the effluent is still extremely hot, the method and apparatus for injecting the compositions into the effluent remains the subject of an intense search.
- a treatment fluid e.g., an aqueous solution of a NO x reducing composition into an effluent of the combustion of a carbonaceous fuel, allowing for independent variability of droplet size and spray parameters.
- a process and apparatus for reducing the concentration of pollutants, such as nitrogen oxides, in an effluent from the combustion of a carbonaceous fuel are presented.
- the process comprises: providing an atomization conduit which extends into the effluent from the combustion of a carbonaceous fuel; providing a supply conduit coaxial with and axially slidable within the atomization conduit; supplying an effluent treatment fluid through the supply conduit to inject the fluid into the effluent; and supplying an atomization fluid through the atomization conduit to effect atomization of the solution and to disperse the solution throughout the effluent.
- the apparatus comprises a probe for the supply of an atomized treatment fluid into an effluent from the combustion of a fuel, comprising: (a) an atomization conduit which extends into an effluent from the combustion of a fuel; (b) means for supplying an atomization fluid to said atomization conduit; (c) a supply conduit coaxial with and axially slidable within said atomization conduit; and (d) means for supplying a metered amount of an effluent treatment fluid through said supply conduit to inject said treatment fluid into said effluent; wherein the axial position of said supply conduit in relation to the end of said atomization conduit and the rate of supply of said atomization fluid may be selected to provide droplets of varying sizes and distance of injection of said droplets throughout said effluent.
- the axial slidability of the supply conduit which can be adjusted in concert with the rate of supply of the atomization fluid, provides the independent selection of treatment solution droplet size and allows the adequate dispersal of the treatment fluid throughout the effluent to reduce the concentration of nitrogen oxides in the effluent.
- FIG. 1 is an installation schematic in perspective, partially broken away, of the apparatus of the present invention disposed in a utility boiler;
- FIG. 2 is a side elevation view, partially broken away of the apparatus of the present invention wherein the portion of the supply conduit is partially retracted;
- FIG. 3 is a partial side elevation view of the apparatus of the present invention wherein the portion of the supply conduit is extended;
- FIG. 4 is a front cross-sectional view, taken across line 4--4 in FIG. 2, of the supply and atomization conduits of the present invention
- FIG. 5 is a side elevation view of an alternate embodiment of the apparatus of the present invention.
- FIG. 6 is a front cross-sectional view, taken along line 6--6 in FIG. 5, of the embodiment of the apparatus of the present invention illustrated in FIG. 4.
- This invention relates to a process and apparatus for reducing the concentration of nitrogen oxides, or other pollutants, in an effluent from the combustion of a carbonaceous fuel.
- the term "front” refers to the end of the apparatus which extends into the effluent; the term “rear” refers to the end of the apparatus from which the fluids and solutions may be supplied.
- the apparatus 20 of this invention comprises a probe 21 comprising a supply conduit 24 which is operable to supply and inject a treatment fluid 28, such as a solution, into a high temperature environment, such as the effluent stream of a utility boiler 10.
- Supply conduit 24 may be any suitable conduit for this purpose and is advantageously a seamless tube of a temperature and corrosion resistant material such as a metal, especially temperature-resistant stainless steel.
- Fluid 28 to be injected through supply conduit 24 is supplied by any conventional supply or pumping device (not shown), as would be familiar to the skilled artisan, and is preferably supplied through a metering device to allow careful control of the amount of fluid injected.
- Fluid 28 to be injected typically comprises a solution having at least one additive compound effective in reducing NO x and/or SO x under the conditions of injection. It can, however, be a fluidized particulate material.
- the direction of flow of the effluent is shown by arrows 60.
- the temperature of the effluent at the point of injection, the concentration of the additive compound in the solution, and the size of the droplets in the dispersion, are selected to achieve reduction in nitrogen oxide or other pollutant levels in the effluent.
- a preferred embodiment of the invention provides for introducing an aqueous treatment solution, such as urea alone as described in copending and commonly assigned U.S. patent application, Ser. No. 784,826 filed Oct.
- urea as employed in this description includes the compound urea itself, as well as compounds equivalent in effect.
- the compounds are ammonium carbonate, ammonium formate, ammonium oxalate, ammonium hydroxide and various stable amines, and mixtures of two or more of these or one or more of these with various enhancers.
- enhancers are compounds selected from the group consisting of guanidine, guanidine carbonate, biguanide, guanylurea sulfate, melamine, dicyandiamide, calcium cyanamide, biuret, 1,1'-azobisformamide, methylol urea, methylol urea-urea condensation product, dimethylol urea, methyl urea, dimethyl urea, and hexamethylenetetramine (HMTA).
- urea should not be taken as limiting to urea itself but should extend to urea and all of its equivalents. It is pointed out that the term equivalent is not limited to exact equivalents, and various materials within the listing of equivalents will be optimally operable at some conditions which are different than those for others of the listed materials. Moreover, some of the materials may be more effective than others.
- Aqueous solutions are typical due to their economy and can be employed with suitable effectiveness in many situations.
- the effective solutions will vary from saturated to dilute. While water will be an effective solvent for most applications, there are instances where other solvents may be advantageous in combination with water.
- Injection is preferably done at a plurality of spaced positions, as illustrated in FIG. 1, and at a distribution of droplet sizes within the range of about 10 to about 10,000 microns Sauter mean diameter. It is an advantage of this invention that wide variations of droplet sizes within this broad range can be achieved along with uniform mixing of the additive compound within the effluent. Droplets can be fine (less than 100 microns), medium (100-500 microns) or coarse (greater than 500 microns) with distance of injection varied from a few feet to as great as 15 feet or more as is required by the particular system. With this degree of flexibility in injection pattern formation and substantially infinite variability of droplet size, it is possible to rapidly and effectively adjust the operation to effluent flows from combustors of widely varying design and conditions of operation. Thus, the injection pattern and distribution of droplet sizes allows uniform dispersion of active material throughout the effluent because some droplets will evaporate immediately adjacent the injection apparatus, while others will survive and release active material on the far side of the boiler or other effluent passage and downstream.
- Droplet sizes are determined with a Malvern 2200 instrument, utilizing a Franhofer diffraction, laser-based system. And, unless otherwise indicated, all parts and percentages are based on the weight of the composition at the particular point of reference.
- Treatment fluid 28 should be dispersed uniformly within effluent stream 60 at a point where effluent 60 is at a temperature effective for pollutant reduction employing the desired additive at a particular concentration and droplet size.
- the temperature will be above about 1300° F. with enhancers, and above about 1550° F. in the absence of enhancers.
- large industrial boilers 10 of the type employed for utility power plants and other large facilities will typically be water jacketted and have water tubes 40, allowing access only at limited points.
- the interior of boiler 10 can be accessed only in the area of the flame 15 and at an area above the flame, where the temperatures at full load are typically within the range of about 2200° F. to about 2600° F.
- the temperature at these points of access will typically fall within the range of about 2100° F. to about 2600° F., and when fired with coal or oil, will typically fall within the range of about 2050° F. to 2400° F.
- Treatment fluid 28 is preferably injected at a number of spaced positions, as illustrated in FIG. 1, in a manner effective to uniformly form and disperse droplets of fluid 28 within the flowing effluent stream 60 to achieve uniform mixing.
- the concentration of the additive compound or compounds within effluent 60 should be sufficient to provide a reduction in nitrogen oxide, sulfur oxide, or other designated pollutant levels.
- the active compound will be employed at a molar ratio of nitrogen in the additive compound to the baseline nitrogen oxide level of about 1:10 to 2:1, and will more preferably be within the range of about 1:4 to 3:2.
- concentration of this component will depend upon the overall economics of the process, and must further take into account the effect it has on the size of the droplets, the ability to uniformly disperse the droplets, and the life of the droplets within effluent 60 under the high temperature conditions existing therein.
- Probe 21 of this invention further comprises an atomization conduit 30, as illustrated in FIG. 3, for supply of an atomization fluid 32.
- Atomization conduit 30 may be any suitable conduit operable to supply atomization fluid 32 and is advantageously a seamless tube of a temperature resistant material such as a metal, especially temperature-resistant stainless steel.
- Atomization fluid 32 to be supplied through atomization conduit 30 may be any fluid operable to cause atomization of treatment fluid 28 supplied through supply conduit 24.
- atomization fluid 32 is steam or a gas, such as air, which is supplied to atomization conduit 30 from conventional means (not shown) through, illustratively, valve 34 and fitting 38, the flow of which may be measured by gauge 36.
- atomization fluid 32 is steam.
- Atomization fluid 32 is advantageously supplied at a velocity sufficient to project at least a portion of the droplets of treatment fluid 28 to a distance of at least about 75% of the width of the flue gas passage at the point of injection, as illustrated in FIG. 1.
- Supply conduit 24 is coaxial with and disposed within atomization conduit 30. Further, supply conduit 24 is axially slidable within atomization conduit 30 so that end portion 24a of supply conduit 24 can extend beyond the end 31 of atomization conduit 30, as illustrated in FIGS. 2 and 3, or portion 24a of supply conduit 24 can be retracted into atomization conduit 30, as illustrated in phantom lines in FIG. 3.
- the axial slidability of supply conduit 24 facilitates the independent control of both atomization, i.e., droplet size, and dispersion of fluid 28 throughout effluent 60, i.e., distance of injection. Both of these, along with the flow pattern of the effluent 60 and its temperature, will determine the degree of mixing of the additive with the effluent.
- supply conduit 24 can be slidably adjusted such that it is retracted into atomization conduit 30 by about 0.5 inches or such that portion 24a of supply conduit 24 extends about 0.5 inches beyond end 31 of atomization conduit 30.
- Such axial slidability of supply conduit 24 can be provided by suitable means known to the skilled artisan, such as by compression fitting 26 illustrated in FIG. 2.
- Atomization is a function of the force of atomization fluid 32 contacting solution 28 as it exits the front end of supply conduit 24.
- the force of atomization fluid 32 contacting fluid 28 can be varied by varying the flow of atomization fluid 32 through atomization conduit 30 or by adjusting the length of portion 24a of supply conduit 24 which extends beyond end 31 of atomization conduit 30. For instance, the greater the flow of atomization fluid 32 through atomization conduit 30, the greater the atomization; the shorter the length of portion 24a of supply conduit 24 extending beyond end 31 of atomization conduit 30 or, when end portion 24a of supply conduit 24 is retracted into atomization conduit 30, the greater the atomization.
- the dispersion of fluid 28 throughout effluent 60 is also a function of the force of atomization fluid 32 contacting fluid 28 as it exits the front end of supply conduit 24.
- a significant advantage of this invention is the ability to optimize both atomization and dispersion. For example, if lesser atomization, i.e., larger droplet size, yet greater dispersion is desired, the flow of atomization fluid 32 and length of portion 24a of supply conduit 24 which extends beyond end 31 of atomization conduit 30 can be adjusted to provide these two characteristics.
- the flow of atomization fluid 32 serves to prevent any particles which precipitate from fluid 28 from collecting at the end of supply conduit 24 from where they might otherwise break off as a chunk and cause damage to the inside of boiler 10.
- the flow of atomization fluid 32 also serves to cool supply conduit 24 to reduce the chances of supply conduit 24 failure due to the high temperature environment of boiler 10.
- probe 21 of this invention may be provided with alignment tabs 23 to maintain supply conduit 24 centrally disposed within atomization conduit 30.
- Alignment tabs 23 may be placed intermittently along the length of probe 24 or comprise fins disposed along the entire length of probe 21, although fins are not preferred due to the possibility of their influence on the flow of atomization fluid 32.
- Alignment tabs 23 are preferably disposed on either the inside of atomization conduit 30, or, more preferably, the outside of supply conduit 24 and are advantageously attached by welding. It is important to note that if alignment tabs 23 are attached to both the inside of atomization conduit 30 and the outside of supply conduit 24, the axial slidability of supply conduit 24 will be prevented.
- probe 121 is provided with a cooling conduit 150 disposed outside of and around a portion of atomization conduit 130.
- An appropriate cooling fluid 158 such as air, water or steam, may be circulated or flowed through cooling conduit 150 to maintain the cooling of both atomization and supply conduits 130 and 124 in the high temperature environment of a boiler.
- Cooling fluid 158 may be supplied to cooling conduit 150 from a suitable source (not shown) through, illustratively, appropriate valve 153 and fitting 159, and measured by gauge 152, as would be familiar to the skilled artisan.
- alignment tabs 154 may also be provided between atomization conduit 130 and cooling conduit 150 as illustrated in FIG. 6.
- This Example illustrates the reduction of NO x concentration in an effluent and degree of control of droplet size which may be achieved using the process and apparatus of the present invention.
- the burner used is a burner having an effluent flue conduit, known as a flame tube, approximately 209 inches in length and having an internal diameter of 8 inches and walls 2 inches thick.
- the burner has a flame area adjacent the effluent entry port and flue gas monitors adjacent the effluent exit port to measure the concentration of compositions such as nitrogen oxides, sulfur oxides, ammonia, carbon monoxide, and other compounds of interest present in the effluent.
- the effluent flue conduit additionally has a thermocouple for temperature measurement.
- a probe of the present invention having a supply conduit with an outside diameter of about 1/16 inch and an atomization conduit having an outside diameter of about 1/4 inch is inserted through a port in the wall of the flame tube at a position adjacent a thermocouple. The probe is inserted such that the atomization conduit extends about 3 inches into the interior of the flame tube.
- a treatment fluid is prepared by mixing a solution comprising 50% by weight of urea, 49% by weight of water and 1% by weight of a commercial surfactant, with water to obtain 10% by weight solution of urea.
- the treatment fluid is supplied through the supply conduit at a rate of 200 ml/hr. at an effluent temperature of 1765° F.
- the temperature measured 43 inches downstream is 1570° F. and 40 inches further downstream is 1330° F.
- the supply conduit is adjusted so that its end portion is withdrawn approximately 1/4 inch from the end of the atomization conduit, and the flow of air, used as atomization fluid, is set at 45 standard liters per minute.
- the effluent NO x concentration measured after treatment as described is 97 ppm, a reduction in NO x concentration of 46.7%.
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- Treating Waste Gases (AREA)
Abstract
Description
TABLE 1 ______________________________________ Size (Microns) % Under* % In Band** ______________________________________ 100.0 100.0 0.0 95.9 100.0 0.3 82.7 99.7 3.8 71.4 95.9 2.5 61.6 93.4 0.0 53.1 93.4 4.1 45.8 89.4 7.1 39.5 82.2 14.0 34.1 68.2 22.3 29.4 45.9 17.9 25.4 28.0 10.0 21.9 18.0 8.7 18.9 9.2 5.6 16.3 3.6 2.5 14.1 1.2 0.7 12.1 0.4 0.0 10.5 0.4 0.0 9.0 0.4 0.0 7.8 0.4 0.0 6.7 0.4 0.0 5.8 0.4 0.0 ______________________________________ *Refers to the percentage of droplets which are measured as having a size below the indicated size. **Refers to the percentage of droplets which are measured as having a siz between the indicated size and the next lower size.
Claims (9)
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/009,696 US4842834A (en) | 1987-02-02 | 1987-02-02 | Process for reducing the concentration of pollutants in an effluent |
| AU12972/88A AU593983B2 (en) | 1987-02-02 | 1988-02-02 | Process & apparatus for reducing the concentration of pollutants in an effluent |
| EP19880902016 EP0300028A4 (en) | 1987-02-02 | 1988-02-02 | METHOD AND INSTALLATION FOR REDUCING THE CONCENTRATION OF POLLUTANTS IN AN EFFLUENT. |
| PCT/US1988/000300 WO1988005762A1 (en) | 1987-02-02 | 1988-02-02 | Process and apparatus for reducing the concentration of pollutants in an effluent |
| JP63501912A JPH01502495A (en) | 1987-02-02 | 1988-02-02 | Method and apparatus for reducing pollutant concentration in runoff pollutants |
| NO884370A NO884370L (en) | 1987-02-02 | 1988-09-30 | PROCEDURE AND APPARATUS FOR AA REDUCE THE CONCENTRATION OF POLLUTANTS IN A DRAINAGE. |
| FI884495A FI884495A0 (en) | 1987-02-02 | 1988-09-30 | FOERFARANDE OCH ANORDNING FOER REDUCERING AV FOERORENINGSKONCENTRATION I AVFALLSVATTEN. |
| DK546588A DK546588A (en) | 1987-02-02 | 1988-09-30 | PROCEDURE AND APPARATUS FOR REDUCING THE CONCENTRATION OF POLLUTANTS IN A DISCHARGE FLOW |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/009,696 US4842834A (en) | 1987-02-02 | 1987-02-02 | Process for reducing the concentration of pollutants in an effluent |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4842834A true US4842834A (en) | 1989-06-27 |
Family
ID=21739181
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/009,696 Expired - Lifetime US4842834A (en) | 1987-02-02 | 1987-02-02 | Process for reducing the concentration of pollutants in an effluent |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US4842834A (en) |
| EP (1) | EP0300028A4 (en) |
| JP (1) | JPH01502495A (en) |
| AU (1) | AU593983B2 (en) |
| FI (1) | FI884495A0 (en) |
| WO (1) | WO1988005762A1 (en) |
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| US5645756A (en) * | 1988-04-29 | 1997-07-08 | Nalco Fuel Tech | Hardness suppression in urea solutions |
| US5045292A (en) * | 1988-09-27 | 1991-09-03 | Von Roll Ag | Process for the removal of nitric oxides from flue gases |
| US4985218A (en) * | 1989-03-03 | 1991-01-15 | Fuel Tech, Inc. | Process and injector for reducing the concentration of pollutants in an effluent |
| US5342592A (en) * | 1989-07-04 | 1994-08-30 | Fuel Tech Europe Ltd. | Lance-type injection apparatus for introducing chemical agents into flue gases |
| US5344628A (en) * | 1989-10-24 | 1994-09-06 | Martin Gmbh Fur Umwelt-Und Energietechnik | Method for introducing and metering a liquid treatment medium in combustion processes |
| US5562884A (en) * | 1990-04-17 | 1996-10-08 | A. Ahlstrom Corporation | Reducing N2 O emissions when burning nitrogen-containing fuels in fluidized bed reactors |
| WO1992002290A1 (en) * | 1990-07-27 | 1992-02-20 | Aalborg Ciserv International A/S | Method and apparatus for reducing the contents of nitrogen oxides in combustion effluent gas |
| US5543123A (en) * | 1990-08-01 | 1996-08-06 | Nalco Fuel Tech | Low pressure formation of a urea hydrolysate for nitrogen oxides reduction |
| US5443805A (en) * | 1991-08-21 | 1995-08-22 | Massachusetts Institute Of Technology | Reduction of combustion effluent pollutants |
| US6432373B1 (en) * | 1992-03-27 | 2002-08-13 | Tokyo Gas Co., Ltd. | Method for removing nitrogen oxides from exhaust gas |
| WO1994002410A1 (en) * | 1992-07-24 | 1994-02-03 | Nalco Fuel Tech | BOILER OPERATION WITH DECREASED NOx AND WASTE WATER DISCHARGE |
| WO1994008893A1 (en) * | 1992-10-13 | 1994-04-28 | Nalco Fuel Tech | Process and composition for pollution control |
| WO1994008895A1 (en) * | 1992-10-13 | 1994-04-28 | Nalco Fuel Tech | Process and composition for pollution control |
| US5536482A (en) * | 1992-10-13 | 1996-07-16 | Nalco Fuel Tech | Process for pollution control |
| US5489419A (en) * | 1992-10-13 | 1996-02-06 | Nalco Fuel Tech | Process for pollution control |
| US5478542A (en) * | 1992-11-23 | 1995-12-26 | Nalco Fuel Tech | Process for minimizing pollutant concentrations in combustion gases |
| US5326536A (en) * | 1993-04-30 | 1994-07-05 | The Babcock & Wilcox Company | Apparatus for injecting NOx inhibiting liquid reagent into the flue gas of a boiler in response to a sensed temperature |
| US6190628B1 (en) * | 1993-04-30 | 2001-02-20 | Diamond Power International, Inc. | Method for injecting NOx inhibiting liquid reagent into the flue gas of a boiler in response to a sensed temperature |
| US5453258A (en) * | 1993-05-08 | 1995-09-26 | Bayer Aktiengesellschaft | Method of removing nitrogen oxides from hot flue gases |
| US5315941A (en) * | 1993-06-07 | 1994-05-31 | The Babcock & Wilcox Company | Method and apparatus for injecting nox inhibiting reagent into the flue gas of a boiler |
| US6210650B1 (en) * | 1993-07-21 | 2001-04-03 | Andritz-Patentverwaltungs-Gesellschaft M.B.H | Process for regenerating hydrochloric acid from pickling plants |
| US5404841A (en) * | 1993-08-30 | 1995-04-11 | Valentine; James M. | Reduction of nitrogen oxides emissions from diesel engines |
| US5489420A (en) * | 1994-03-10 | 1996-02-06 | Nalco Fuel Tech | Nitrogen oxides reducing agent and a phosphate |
| US5462718A (en) * | 1994-06-13 | 1995-10-31 | Foster Wheeler Energy Corporation | System for decreasing NOx emissions from a fluidized bed reactor |
| US5728357A (en) * | 1996-04-10 | 1998-03-17 | Nalco Fuel Tech | Reduction of NOx emissions from rotary cement kilns by selective noncatalytic reduction |
| US5681536A (en) * | 1996-05-07 | 1997-10-28 | Nebraska Public Power District | Injection lance for uniformly injecting anhydrous ammonia and air into a boiler cavity |
| US5976475A (en) * | 1997-04-02 | 1999-11-02 | Clean Diesel Technologies, Inc. | Reducing NOx emissions from an engine by temperature-controlled urea injection for selective catalytic reduction |
| US5968464A (en) * | 1997-05-12 | 1999-10-19 | Clean Diesel Technologies, Inc. | Urea pyrolysis chamber and process for reducing lean-burn engine NOx emissions by selective catalytic reduction |
| US6203770B1 (en) | 1997-05-12 | 2001-03-20 | Clean Diesel Technologies, Inc. | Urea pyrolysis chamber and process for reducing lean-burn engine NOx emissions by selective catalytic reduction |
| US6125629A (en) * | 1998-11-13 | 2000-10-03 | Engelhard Corporation | Staged reductant injection for improved NOx reduction |
| EP1085265A1 (en) * | 1999-09-17 | 2001-03-21 | Kemter, Andreas | Injection lance for introducing liquid or gaseous media into a flue gas flow |
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Also Published As
| Publication number | Publication date |
|---|---|
| JPH01502495A (en) | 1989-08-31 |
| WO1988005762A1 (en) | 1988-08-11 |
| FI884495A7 (en) | 1988-09-30 |
| EP0300028A1 (en) | 1989-01-25 |
| FI884495A0 (en) | 1988-09-30 |
| EP0300028A4 (en) | 1990-02-05 |
| AU593983B2 (en) | 1990-02-22 |
| AU1297288A (en) | 1988-08-24 |
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